Fetal hemoglobin silencing in humans

Interruption of the normal fetal-to-adult transition of hemoglobin expression should largely ameliorate sickle cell and beta-thalassemia syndromes. Achievement of this clinical goal requires a robust understanding of gamma-globin gene and protein silencing during human development. For this purpose,...

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Bibliografische gegevens
Hoofdauteurs: Oneal, Patricia A., Gantt, Nicole M., Schwartz, Joseph D., Bhanu, Natarajan V., Lee, Y. Terry, Moroney, John W., Reed, Christopher H., Schechter, Alan N., Luban, Naomi L. C., Miller, Jeffery L.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: The American Society of Hematology 2006
Onderwerpen:
Red Cells
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1895549/
https://ncbi.nlm.nih.gov/pubmed/16735596
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2006-04-015859
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